Suzanne de Bruijn

145 A RIPOR2 deletion is a frequent cause of adult-onset hearing loss 16. Diaz-Horta, O., Subasioglu-Uzak, A., Grati, M.h., DeSmidt, A., Foster, J., Cao, L. et al. FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing. Proceedings of the National Academy of Sciences of the United States of America 111 , 9864-9868 (2014). 17. De Brouwer, A.P.M., Kunst, H.P.M., Krebsova, A., van Asseldonk, K., Reis, A., Snoeckx, R.L. et al. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3. American Journal of Medical Genetics Part A 137A , 41-46 (2005). 18. Kunst, H., Marres, H., Huygen, P., Van Duijnhoven, G., Krebsova, A., Van der Velde, S. et al. Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21). Clinical Otolaryngology & Allied Sciences 25 , 45-54 (2000).